학술논문

A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children
Document Type
article
Source
npj Science of Learning, Vol 9, Iss 1, Pp 1-18 (2024)
Subject
Special aspects of education
LC8-6691
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Language
English
ISSN
2056-7936
Abstract
Abstract Dyslexia and developmental language disorders are important learning difficulties. However, their genetic basis remains poorly understood, and most genetic studies were performed on Europeans. There is a lack of genome-wide association studies (GWAS) on literacy phenotypes of Chinese as a native language and English as a second language (ESL) in a Chinese population. In this study, we conducted GWAS on 34 reading/language-related phenotypes in Hong Kong Chinese bilingual children (including both twins and singletons; total N = 1046). We performed association tests at the single-variant, gene, and pathway levels. In addition, we tested genetic overlap of these phenotypes with other neuropsychiatric disorders, as well as cognitive performance (CP) and educational attainment (EA) using polygenic risk score (PRS) analysis. Totally 5 independent loci (LD-clumped at r2 = 0.01; MAF > 0.05) reached genome-wide significance (p 0.3 and having at least 2 correlated SNPs (r2 > 0.5) with p